Paclitaxel Magnetic Core⁻Shell Nanoparticles Based on Poly(lactic acid) Semitelechelic Novel Block Copolymers for Combined Hyperthermia and Chemotherapy Treatment of Cancer.
Evi ChristodoulouMaria NerantzakiStavroula NanakiPanagiotis BarmpalexisKleoniki GiannousiCatherine Dendrinou-SamaraMakis AngelakerisEleni GounariAntonios D AnastasiouDimitrios N BikiarisPublished in: Pharmaceutics (2019)
Magnetic hybrid inorganic/organic nanocarriers are promising alternatives for targeted cancer treatment. The present study evaluates the preparation of manganese ferrite magnetic nanoparticles (MnFe2O4 MNPs) encapsulated within Paclitaxel (PTX) loaded thioether-containing ω-hydroxyacid-co-poly(d,l-lactic acid) (TEHA-co-PDLLA) polymeric nanoparticles, for the combined hyperthermia and chemotherapy treatment of cancer. Initially, TEHA-co-PDLLA semitelechelic block copolymers were synthesized and characterized by 1H-NMR, FTIR, DSC, and XRD. FTIR analysis showed the formation of an ester bond between the two compounds, while DSC and XRD analysis showed that the prepared copolymers were amorphous. MnFe2O4 MNPs of relatively small crystallite size (12 nm) and moderate saturation magnetization (64 emu·g-1) were solvothermally synthesized in the sole presence of octadecylamine (ODA). PTX was amorphously dispersed within the polymeric matrix using emulsification/solvent evaporation method. Scanning electron microscopy along with energy-dispersive X-ray spectroscopy and transmission electron microscopy showed that the MnFe2O4 nanoparticles were effectively encapsulated within the drug-loaded polymeric nanoparticles. Dynamic light scattering measurements showed that the prepared nanoparticles had an average particle size of less than 160 nm with satisfactory yield and encapsulation efficiency. Diphasic PTX in vitro release over 18 days was observed while PTX dissolution rate was mainly controlled by the TEHA content. Finally, hyperthermia measurements and cytotoxicity studies were performed to evaluate the magnetic response, as well as the anticancer activity and the biocompatibility of the prepared nanocarriers.
Keyphrases
- electron microscopy
- drug delivery
- cancer therapy
- lactic acid
- drug release
- high resolution
- molecularly imprinted
- papillary thyroid
- magnetic nanoparticles
- walled carbon nanotubes
- magnetic resonance
- ionic liquid
- photodynamic therapy
- young adults
- squamous cell
- emergency department
- high intensity
- solid state
- locally advanced
- mass spectrometry
- computed tomography
- single molecule
- magnetic resonance imaging
- smoking cessation
- adverse drug
- room temperature
- lymph node metastasis
- electronic health record
- water soluble